chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139172736791727368AG24GENIChomozygous114577550
139172844591728446TA16GENIChomozygous115153410
139172984491729847GAA21GENIChomozygous134736093
139173147691731477TC27GENIChomozygous114577552
139173311791733118TC21GENIChomozygous114577554
139173336891733369AG9GENIChomozygous114577560
139173357391733573A16GENIChomozygous131134655
139173411791734120AAG5GENIChomozygous131134656
139173484091734841TC15GENIChomozygous115153412
139173614891736149AC13GENIChomozygous114577572
139173619891736199CT2GENIChomozygous131511916
139173637391736373T3GENIChomozygous129085096
139173638091736381AT3GENIChomozygous114424506
139173638191736382GA3GENIChomozygous114424508
139173638591736386A4GENIChomozygous129085097
139173639991736400GC5GENIChomozygous114577574
139173640791736408AC6GENIChomozygous114577576
139173640891736409CA6GENIChomozygous114577578
139173643491736434G10GENIChomozygous129085098
139173651191736512G22GENIChomozygous129085099
139173651691736516G22GENIChomozygous129085100
139173652991736529C20GENIChomozygous129085101
139173655491736555C18GENIChomozygous129085102
139173657891736579A18GENIChomozygous129085103
139173658891736588T15GENIChomozygous129085104
139173659291736595AGT15GENIChomozygous129085105
139173659991736600C15GENIChomozygous129085106
139173663591736635GT16GENIChomozygous129085107
139173664491736645A15GENIChomozygous129085108
139173664591736646AC15GENIChomozygous114424510
139173665591736656C17GENIChomozygous129085109
139173666091736661G18GENIChomozygous129085110
139173696291736962T16GENIChomozygous134736094